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Dive into the research topics where Mohamad Qari is active.

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Featured researches published by Mohamad Qari.


Thrombosis and Haemostasis | 2007

Reduction of painful vaso-occlusive crisis of sickle cell anaemia by tinzaparin in a double-blind randomized trial.

Mohamad Qari; Soad K. Al-Jaouni; Mohamad Salleh Alardawi; Huda Fatani; Fatin Mohamad Alsayes; Panagiotis Zografos; Mohamad Alsaigh; Adnan Alalfi; Mohamad Alamin; Abdulilah Gadi; Shaker A. Mousa

A randomized double-blind clinical trial was performed to test the safety and efficacy of a low-molecular-weight heparin, tinzaparin (Innohep), for the management of acute painful vasoocclusive crisis characteristic of sickle cell anemia (SCA). We studied 253 patients with acute painful crisis but with no other complications of SCA, randomized to treatment or control groups. In the treatment group, 127 patients received tinzaparin at 175 IU/kg, subcutaneous once daily, along with supportive care including morphine analgesia; in the control group, 126 patients received placebo and the same supportive care. The maximal experimental treatment period was seven days. Analysis revealed a statistically significant reduction in number of days with the severest pain score, overall duration of painful crisis, and duration of hospitalization (p < 0.05 for each comparison of tinzaparin vs. placebo). The decline in pain intensity was sharper for tinzaparin-treated patients, and complications consisted of two minor bleeding events that were reported and treated by cessation of tinzaparin. This investigation demonstrated that tinzaparin, administered at its approved treatment regimen, reduced the severity and duration of acute crisis of SCA.


Methods of Molecular Biology | 2010

Diagnosis and Management of Sickle Cell Disorders

Shaker A. Mousa; Mohamad Qari

Sickle cell disease (SCD) is a wide-spread inherited hemolytic anemia that is due to a point mutation leading to a valine/glutamic acid substitution in the beta-globin chain, causing a spectrum of clinical manifestations in addition to hemolysis and anemia. Acute painful crisis is a common sequela that can cause significant morbidity and negatively impact the patients quality of life. Remarkable improvements in our understanding of the pathogenesis of this clinical syndrome and the role of cell adhesion, inflammation, and coagulation in acute painful crisis have led to changes in the management of pain. Due to the endemic nature of SCD in various parts of the Middle East, a group of physicians and scientists from the United States and Middle East recently met to draw up a set of suggested guidelines for the management of acute painful crisis that are reflective of local and international experience. This chapter brings together a detailed etiology, pathophysiology, and clinical presentation of SCD, including the differential diagnoses of pain associated with the disease, with evidence-based recommendations for pain management and the potential impact of low-molecular weight heparin (LMWH), from the perspective of physicians and scientists with long-term experience in the management of a large number of SCD patients.


Pediatric Blood & Cancer | 2014

Deviating from safety guidelines during deferiprone therapy in clinical practice may not be associated with higher risk of agranulocytosis

Mohssen S. Elalfy; Yasser Wali; Mohamad Qari; Ghazi A. Damanhouri; Youssef Al-Tonbary; Dilek Yazman; Zakaria Al Hawsawi; Zeynep Karakas; Yurdanur Kilinç; M. Akif Yesilipek; Mohamed Badr; Usama R. Elsafy; Mostafa Salama; Yousryeia Abdel Rahman; Shebl Said Shebl; Anne Stilman; Noemi Toiber Temin; Fernando Tricta

A risk associated with the iron chelator deferiprone is the development of neutropenia or agranulocytosis. Accordingly, the product label recommends weekly blood monitoring and immediate interruption of treatment upon detection of an absolute neutrophil count (ANC) <1.5u2009×u2009109/L, out of concern that continued therapy might lead to a more severe drop. However, it is uncertain how these recommendations are followed under real‐life conditions and, if they are not followed, whether continuation of therapy results in increased incidence of agranulocytosis.


Saudi Journal of Biological Sciences | 2017

Antimicrobial effect of different types of honey on Staphylococcus aureus

Saad B. Almasaudi; Alaa A.M. Al-Nahari; El Sayed M. Abd El-Ghany; Elie K. Barbour; Saad M. Al Muhayawi; Soad K. Al-Jaouni; Esam I. Azhar; Mohamad Qari; Yousef Qari; Steve Harakeh

Honey exhibits antimicrobial activities against a wide range of bacteria in different milieu. This study aims to compare the effects of five types of honey (both imported and local Saudi honey) against Staphylococcus aureus. The five types of honey (Manuka Honey UMF +20, Manuka Honey UMF +16, Active +10 Manuka Honey, Sidr honey and Nigella sativa honey) were evaluated for their bactericidal/bacteriostatic activities against both methicillin resistant and sensitive S. aureus. The inhibitory effect of honey on bacterial growth was evident at concentrations of 20% and 10% (v/v). Manuka Honey showed the best results. Manuka Honey UMF +20 had a bactericidal effect on both methicillin resistant and sensitive S. aureus. However, Sidr and N. sativa honey exerted only a bacteriostatic effect. The efficacy of different types of honey against S. aureus was dependent on the type of honey and the concentration at which it was administered. Manuka Honey had the best bactericidal activity. Future experiments should be conducted to evaluate the effects of honey on bacterial resistance.


Orphanet Journal of Rare Diseases | 2013

Regional consensus opinion for the management of Beta thalassemia major in the Arabian Gulf area

Mohamad Qari; Yasser Wali; Muneer H Albagshi; Mohammad Alshahrani; Azzah Alzahrani; Ibrahim Al-Hijji; Abdul-Kareem Al-Momen; Abdullah Aljefri; Hussain H Al Saeed; Shaker Abdullah; Ahmad Al Rustumani; Khoutir Mahour; Shaker A. Mousa

Thalassemia syndrome has diverse clinical presentations and a global spread that has far exceeded the classical Mediterranean basin where the mutations arose. The mutations that give rise to either alpha or beta thalassemia are numerous, resulting in a wide spectrum of clinical severity ranging from carrier state to life-threatening, inherited hemolytic anemia that requires regular blood transfusion. Beta thalassemia major constitutes a remarkable challenge to health care providers. The complications arising due to the anemia, transfusional iron overload, as well as other therapy-related complications add to the complexity of this condition. To produce this consensus opinion manuscript, a PubMed search was performed to gather evidence-based original articles, review articles, as well as published work reflecting the experience of physicians and scientists in the Arabian Gulf region in an effort to standardize the management protocol.


Hemoglobin | 2011

FLOW CYTOMETRIC ASSESSMENT OF LEUKOCYTE FUNCTION IN SICKLE CELL ANEMIA

Mohamad Qari; Wed A. Zaki

Sickle cell anemia is associated with susceptibility to infection due to hyposplenism and the reduced ability of neutrophils to kill pathogenic organisms. In this study, blood samples from sickle cell anemia patients were divided into two groups: the painful crisis group and the steady state group. Flow cytometric assessment of phagocytosis and burst formation of neutrophils and monocytes as well as basophil function were performed, and these were compared to those of age- and sex-matched normal control subjects. Neutrophils and monocytes in sickle cell anemia patients were significantly different from those in the normal control subjects in the areas of weaker phagocytosis, fewer ingested bacteria and reduced burst formation. Basophil degranulation was normal. This pilot study using flow cytometry explains in part the susceptibility to infection of sickle cell anemia patients despite their high neutrophil and monocyte counts.


Hemoglobin | 2009

Pattern of HB F Level Rise During Normal Pregnancies

Maha Ibrahim; Mohamad Qari; Wafa Sait; Mansor Abulela

Fetal hemoglobin (Hb F) is the normal hemoglobin (Hb) that is present in the fetus and usually almost absent in adults. The objective of this study was to assess the changes in Hb F levels during normal pregnancy. The level of Hb F was determined in serial blood samples from women at different stages of pregnancy using cation exchange high performance liquid chromatography (HPLC) and compared to age and sex-matched controls. A significant increase (p <0.001) was observed in the level of maternal Hb F; the mean Hb F level during pregnancy was 0.71 ± 0.51%, while in the non pregnant control group it was 0.28 ± 0.35%. There was no significant difference in Hb F levels in the three trimester groups using the ANOVA test (F = 0.25). Correlation studies between the gestational age and level of Hb F showed no significant increase of Hb F with advancing pregnancy (R = −0.053, p >0.05). The cause of the rise in Hb F is yet to be elucidated.


Saudi Medical Journal | 2017

The effect of wet cupping on quality of life of adult patients with chronic medical conditions in King Abdulaziz University Hospital

Soad Al Jaouni; Eman A. El-Fiky; Samiha A. Mourad; Nahla Khamis Ibrahim; Abdullah M. Kaki; Sawsan M. Rohaiem; Mohamad Qari; Laila M. Tabsh; Adel A. Aljawhari

Objectives: To assess the effect of wet cupping on health-related quality of life (HRQOL) of adult patients with chronic medical conditions, who were referred to the Cupping Clinic of King Abdulaziz University Hospital (KAUH), Jeddah, Kingdom of Saudi Arabia. Methods: A controlled, quasi-experimental study design was carried out among 629 patients referred for cupping from the KAUH Specialty Clinics, during the period from January to December 2014. Patients in the intervention group (309 patients) completed a pre-test included WHO quality of life-BREF, received one wet-cupping session, and filled-out the post-test (1 month later). Patients in the control group (320 patients) completed the pre-test during their enrollment in the study and post-test one month later. Both groups received their ordinary treatment. Descriptive and inferential statistics were performed. Results: Pain was the most common cause for cupping referral. After cupping intervention, the mean scores of most of the HRQOL domains, especially the physical domain, improved significantly among patients in the intervention group. The mean total score of physical HRQOL domain was 61.6 ± 13.6 before cupping, and reached 69.7 ± 12.6 after intervention (paired t-test=11.3, p=0.000). Improvements in HRQOL were noticed for almost all types of pain and other medical conditions. Conclusion: There are promising effects in favor of using wet cupping for improving HRQOL of patients with chronic conditions. Cupping is recommended as a complementary treatment modality for chronic medical conditions, especially pain.


Methods in molecular medicine | 2004

Guidelines for diagnosis and treatment of deep venous thrombosis and pulmonary embolism.

Hikmat Abdel-Razeq; Mohamad Qari; Jorgen Kristensen; Hussein Alizeidah; Faisal Alsayegh; Mahmoud Marashi; Abdulaziz H. Alzeer; Omar S Al-Amoudi; Hatem O. Qutub; Abdel-Aziz Al-Humiadi; Steen Husted; Shaker A. Mousa


Journal of Applied Hematology | 2012

Iron Balance in β-thalassemia: Maintaining an Antioxidant / Oxidant Ratio

Heena Patel; Mohamad Qari; Shaker A. Mousa

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Shaker A. Mousa

Albany College of Pharmacy and Health Sciences

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Yasser Wali

Sultan Qaboos University

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Jorgen Kristensen

United Arab Emirates University

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